EP3176195A1 - Mounting foam and its application as an adhesive, sealant, to make coatings or to fill void structures inside - Google Patents

Mounting foam and its application as an adhesive, sealant, to make coatings or to fill void structures inside Download PDF

Info

Publication number
EP3176195A1
EP3176195A1 EP16197508.1A EP16197508A EP3176195A1 EP 3176195 A1 EP3176195 A1 EP 3176195A1 EP 16197508 A EP16197508 A EP 16197508A EP 3176195 A1 EP3176195 A1 EP 3176195A1
Authority
EP
European Patent Office
Prior art keywords
weight
foam
foam according
molecular mass
plasticizers
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP16197508.1A
Other languages
German (de)
French (fr)
Inventor
Tomasz Pawlus
Nina Kulis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SELENA LABS Spz oo
Original Assignee
SELENA LABS Spz oo
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SELENA LABS Spz oo filed Critical SELENA LABS Spz oo
Publication of EP3176195A1 publication Critical patent/EP3176195A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0019Use of organic additives halogenated
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • C09J175/06Polyurethanes from polyesters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/4009Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4018Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/20Heterocyclic amines; Salts thereof
    • C08G18/2081Heterocyclic amines; Salts thereof containing at least two non-condensed heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4205Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
    • C08G18/4208Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4804Two or more polyethers of different physical or chemical nature
    • C08G18/4816Two or more polyethers of different physical or chemical nature mixtures of two or more polyetherpolyols having at least three hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4829Polyethers containing at least three hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4854Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0038Use of organic additives containing phosphorus
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/14Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
    • C08J9/141Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/02Halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • C09J175/08Polyurethanes from polyethers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J5/00Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • C09J5/08Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers using foamed adhesives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2101/00Manufacture of cellular products
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2170/00Compositions for adhesives
    • C08G2170/60Compositions for foaming; Foamed or intumescent adhesives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00Foams characterized by the expanding agent
    • C08J2203/14Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2207/00Foams characterised by their intended use
    • C08J2207/02Adhesive
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • C08J2375/08Polyurethanes from polyethers

Definitions

  • the foam according to the invention is characterised in that polyetherols are selected from the group of polyether triols: propoxylated glycerol, glycerine-based polyoxyalkilenetriol with a functionality of 3 and a molecular mass from 500 to 3,700.
  • the foam according to the invention is characterised in that polyesters are selected from the group of aromatic polyester polyols derived from ethylene polyphthalate. More preferably, the foam according to the invention is characterised in that the ratio of isocyanate groups and hydroxyl groups NCO:OH is from 3.2 to 4.2, more preferably from 3.4 to 3.9.
  • the other object of the invention is the use of the foam defined in any claim 1 to 8 as an adhesive, packing to fix EPS, XPS insulation in ETICS systems and to fix thermal insulation to flat roofs and foundations and to fill void structures inside.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Sealing Material Composition (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The object of the invention is the mounting foam containing polyols, isocyanates, plasticizers, surfactants, a catalyst and gases, characterised in that it contains polyols from 30% to 35%, gases from 15.5% to 17.5%, where the ratio of NCO:OH is from 3.4 to 3.9, and its application as an adhesive, to make coatings or to fill void structures inside

Description

  • The object of the invention is a mounting foam, particularly to fill gaps in the building industry and to fix insulating materials to the structural elements of buildings.
  • Adhesive mortars are known in the building industry to bond insulation element to building walls, the preparation of which requires mixing a dry cement-based composition with water. Additionally, these mortars require from the person preparing them appropriate precision during the preparation of the adhesive mortar while mixing and applying it. Mounting foams are known for direct application from a can with compressed composition. A light adhesive mortar is known from patent application PL376805 for fixing EPS panels in insulation systems made according to the light wet method, consisting of a light mineral filler, preferably perlite or organic filler, preferably expanded polystyrene in a form of granules or beads with a diameter of 0.2-3 mm, preferably in the quantity of 20-70% by volume. A mounting foam is known from patent PL192714 whose base material contains from 35 to 60% of Portland cement, from 65% to 35% of silicate fillers, from 2% to 5% of dispersing powder, from 0.2% to 1% of modifiers and from 0.5% to 3% of aluminium powder. A low-pressure gun foam Tytan 65 made by Selena is known, containing gases, surfactants, polyols and a catalyst. Unfortunately, these foams still have too high foam deflection, too low position correctability, to low apparent density and no possibility to compensate for uneven surfaces. Unexpectedly, the problems mentioned above have been solved by the present invention.
  • The object of the invention is a mounting foam containing polyols, isocyanates, plasticizers, surfactants, a catalyst and gases, characterised in that it contains polyols from 28% to 40% by weight, more preferably from 30% to 35% by weight. Also preferably, the foam according to the invention is characterised in that it contains polyetherols and polyesters from the group of polyols; however, preferably there is from 23% to 32% by weight of polyetherols and from 5% to 8% by weight of polyesters. Preferably, at least three polyetherols with different hydroxyl numbers and a molecular mass from 500 to 3,700 are used:
    1. A. polyetherols with an hydroxyl number from 40 to 80 mg KOH/g and a molecular mass from 3,000 to 3,700;
    2. B. polyetherols with an hydroxyl number from 80 to 180 mg KOH/g and a molecular mass from 800 to 1500;
    3. C. polyetherols with an hydroxyl number from 180 to 280 mg KOH/g and a molecular mass from 500 to 800.
  • Preferably, polyetherols consist of 10-20% of polyetherols A, 70-85% of polyetherols B and 5-10% polyetherols C.
  • More preferably, the foam according to the invention is characterised in that polyetherols are selected from the group of polyether triols: propoxylated glycerol, glycerine-based polyoxyalkilenetriol with a functionality of 3 and a molecular mass from 500 to 3,700. In another equally advantageous embodiment of the invention, the foam according to the invention is characterised in that polyesters are selected from the group of aromatic polyester polyols derived from ethylene polyphthalate. More preferably, the foam according to the invention is characterised in that the ratio of isocyanate groups and hydroxyl groups NCO:OH is from 3.2 to 4.2, more preferably from 3.4 to 3.9. In another embodiment of the invention, the foam is characterised in that the surfactants are selected from the group of organic modified silicone products, e.g. polyether modified polysiloxane copolymer, e.g. Tegostab B 8871 (Evonik); polyether modified polysiloxane, e.g. Dabco SI3501 (Air Products); polyether polydimethylsiloxane copolymer, e.g. Tegostab B 8526 (Evonik); polyether siloxane, e.g. Tegostab B 8951 (Evonik); siloxane polyoxyalkylene copolymer, e.g. Niax silicone L-6164 (Momentive); methylsiloxane polyoxyalkylene copolymer, e.g. Niax silicone L-5348 (Momentive); and their content in the foam is from 1.5% to 3% by weight, more preferably from 1.8% to 2.2% by weight. The foam according to the invention contains plasticizers from 5% to 15%, more preferably from 9% to 11% by weight. In another advantageous embodiment of the invention, the foam is characterised in that the plasticizers are selected from the group containing chlorinated paraffins with a medium chain from 14 to 17 carbon particles and chlorinated phosphates, where chlorinated paraffins C14-17 constitute from 25% to 35% of the plasticizers and chlorinated phosphates constitute from 65% to 75% of the plasticizers. In another advantageous embodiment of the invention, the foam is characterised in that it contains an amine catalyst, 2,2-dimorpholinyldiethyl ether, from 0.2% to 1%, more preferably from 0.2% to 0.7%. In another advantageous embodiment of the invention, the foam is characterised in that it contains gases from 15.5% to 17.5% by weight. The gases are, preferably, selected from the group containing dimethyl ether and isobutane.
  • The other object of the invention is the use of the foam defined in any claim 1 to 8 as an adhesive, packing to fix EPS, XPS insulation in ETICS systems and to fix thermal insulation to flat roofs and foundations and to fill void structures inside.
  • The foam according to the invention is characterised by the very high correctability time from 12 to 20 minutes, very low panel deflection and possibility to compensate for uneven surfaces. What is more, it is characterised by a high apparent density and tensile resistance.
  • Example
  • The content of the foam according to the invention has been presented below.
  • The foam preparation process consists of the following stages:
    • the components listed in claims 1 to 6 are transferred to a vessel;
    • the mixture of polyols, plasticizers, surfactants and a catalyst is mixed in a tightly closed vessel, protected against humidity, at the room temperature of 23 +/-2°C for 15 minutes;
    • the mixture of polyols, plasticizers, surfactants, the catalyst and 4,4'-diphenylmethane diisocyanate with the content of NCO groups from 29 to 31% by weight is introduced into a metal pressure vessel;
    • dimethyl ether and isobutane are introduced into the pressure vessel and then shaken until the mixture of polyols, plasticizers, surfactants and the catalyst with 4,4'-diphenylmethane diisocyanate is completely blended.
  • The primary reaction of obtaining polyurethane foams is the reaction of polyols containing free hydroxyl groups with diisocyanates with the addition of blowing agents. The foam is extruded, in a controlled manner, from the vessel under pressure through the nozzle to the application site. The foam is delivered as a braid which gradually expands and then hardens in atmospheric humidity.
  • The examination of parameters, post-expansion, tack-free time, correctability, panel deflection, apparent density and tensile resistance, was conducted at the room temperature of 23 +/-2°C and humidity of 50 +/-5% RH, according to the European guidelines EOTA TR 46 and applying test methods approved by the FEICA. The foam was applied on the XPS, EPS panel and fixed to the wall made of cellular concrete. Tensile resistance was tested on the ZWICK materials resistance testing machine with the speed of 10 mm/min +/-1.
    Example I Example II Example III Example IV Example V
    Dimethyl ether 77 82 102 85 96
    Isobutane 63 70 83 70 79
    Isocyanate 390 425 348 385 356
    Polyetherol with an hydroxyl number of 40-80 and a molecular mass of 3,000-3, 700 34 45 32 44 28
    Polyetherol with an hydroxyl number of 80-180 and a molecular mass of 800-1,500 181 158 272 195 238
    Polyetherol with an hydroxyl number of 180-280 and a molecular mass of 500-800 11 23 16 21 14
    Polyester 54 80 80 65 70
    Chlorinated paraffin with a medium chain C14-17 37.5 35 15 38.5 27
    Chlorinated phosphates 112.5 65 35 71.5 63
    Silicone stabilisers 30 15 15 18 22
    Amine catalyst 10 2 2 7 7
    TOTAL 1, 000 1,000 1,000 1,000 1, 000
    NCO:OH 3.9 4.2 3.4 3.9 3.2
    Post-expansion (%) 18 20 15 18 15
    Tack-free time (min) 7 7 8 7 8
    Correctability time (min) 15 15 12 15 12
    Panel reflection up to 5% up to 8% up to 5% up to 5% up to 5%
    Apparent density (kg/m3) 30 28 32 30 33
    Resistance to perpendicular tearing with the 8 mm gap (kPa) 120 120 140 120 140
    Explanations to the table
    Isocyanate 4,4'-Diphenylmethane diisocyanate
    Polyetherol with an hydroxyl number of 40-80 and a molecular mass of 3,000-3, 700 Polyoxyalkilenetriol with an hydroxyl number of 47 mg KOH/g and a molecular mass of 3,600, e.g. Rokopol F3600 (Rokita)
    Polyetherol with an hydroxyl number of 80-180 and a molecular mass of 800-1,500 Polyether triol with an hydroxyl number of 160 mg KOH/g and a molecular mass of 1,055, e.g. Petol-160 (Oltchim) Glycerine-based polyoxyalkilenetriol with an hydroxyl number of 160 mg KOH/g and a molecular mass of 1,000, e.g. Rokopol G1000 (Rokita)
    Polyetherol with an hydroxyl number of 180-280 and a molecular mass of 500-800 Polyether triol with an hydroxyl number of 255 mg KOH/g and a molecular mass of 660, e.g. Desmophen V657 (Bayer) Glycerine-based polyoxyalkilenetriol with an hydroxyl number of 235 mg KOH/g and a molecular mass of 700, e.g. Rokopol V700 (Rokita)
    Polyester Aromatic modified polyester, e.g. Stepanpol T-401 (Stepan)
    Amine catalyst 2,2-Dimorpholinyldiethyl ether
    Chlorinated paraffin with a medium chain C14-17 Chlorinated paraffin CPN 45-15 (Fortischem)
    Chlorinated phosphates Chloromethyl ethyl phosphate, e.g. Roflam P (Rokita), TCPP (Prochema)
  • The foam can be used on both plastered surfaces and unclad walls, made of bricks, ceramic blocks or cellular concrete. It is ideal for curved, undulated and irregular surfaces. It allows for levelling out unevenness of up to 15 mm.

Claims (10)

  1. The mounting foam containing polyols, isocyanates, plasticizers, surfactants, a catalyst and gases, characterised in that it contains polyols from 28% by weight to 40% by weight, more preferably from 30% by weight to 35% by weight.
  2. The foam according to claim 1 characterised in that it contains polyetherols and polyesters from the group of polyols, where, preferably, there is from 23% by weight to 32% by weight of polyetherols and from 5% by weight to 8% by weight of polyesters.
  3. The foam according to claim 1 or 2 characterised in that it contains three polyetherols with different hydroxyl numbers and a molecular mass from 500 to 3,700, more preferably the first of them with the hydroxyl number from 40 to 80 mg KOH/g and a molecular mass from 3,000 to 3,700; the second of them with the hydroxyl number from 80 to 180 mg KOH/g and a molecular mass from 800 to 1,500; and the third of them with the hydroxyl number from 180 to 280 mg KOH/g and a molecular mass from 500 to 800.
  4. The foam according to any claim 1 to 3 characterised in that the surfactants are selected from the group of organic modified silicone products containing polyether modified polysiloxane copolymer, polyether modified polysiloxane, polyether polydimethylsiloxane copolymer, polyether siloxane, siloxane polyoxyalkylene copolymer and methylsiloxane polyoxyalkylene copolymer and, preferably, their content in the foam is from 1.5% by weight to 3% by weight, more preferably from 1.8% by weight to 2.2% by weight.
  5. The foam according to any claim 1 to 4 characterised in that it contains plasticizers from 5% by weight to 15% by weight, more preferably from 9% by weight to 11% by weight, more preferably, the plasticizers are selected from the group containing chlorinated paraffins with a medium chain from 14 to 17 carbon particles and chlorinated phosphates, where chlorinated paraffins C14-17 constitute from 25% by weight to 35% by weight of the plasticizers and chlorinated phosphates constitute from 65% by weight to 75% by weight of the plasticizers.
  6. The foam according to any claim 1 to 5 characterised in that the content of the amine catalyst is from 0.2% by weight to 1% by weight, more preferably from 0.2% by weight to 0,7% by weight.
  7. The foam according to any claim from 1 to 6 characterised in that polyetherols are selected from the group of polyether triols: propoxylated glycerol, glycerine-based polyoxyalkilenetriol with a functionality of 3 and a molecular mass from 500 to 3,700.
  8. The foam according to any claim 1 to 7 characterised in that the content of gases is from 14% by weight to 18.5% by weight, more preferably from 15.5% by weight to 17,5% by weight; more preferably, they are selected from the group containing dimethyl ether and isobutane.
  9. The foam according to any claim 1 to 7 characterised in that the ratio of isocyanate groups and hydroxyl groups NCO:OH is from 3.2 to 4.2, more preferably from 3.4 to 3.9.
  10. The application of the foam defined in any claim 1 to 8 as an adhesive, to fix insulation made of EPS, XPS in ETICS systems and to fix thermal insulation to flat roofs and foundations and to fill void structures inside.
EP16197508.1A 2015-12-01 2016-11-07 Mounting foam and its application as an adhesive, sealant, to make coatings or to fill void structures inside Withdrawn EP3176195A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL415002A PL415002A1 (en) 2015-12-01 2015-12-01 Caulking foam and its application as adhesive, sealant, for manufacturing coatings or for filling interiors of hollow structures

Publications (1)

Publication Number Publication Date
EP3176195A1 true EP3176195A1 (en) 2017-06-07

Family

ID=57321116

Family Applications (1)

Application Number Title Priority Date Filing Date
EP16197508.1A Withdrawn EP3176195A1 (en) 2015-12-01 2016-11-07 Mounting foam and its application as an adhesive, sealant, to make coatings or to fill void structures inside

Country Status (9)

Country Link
US (1) US20170152363A1 (en)
EP (1) EP3176195A1 (en)
CN (1) CN106810662A (en)
AR (1) AR106871A1 (en)
BR (1) BR102016027643A2 (en)
CA (1) CA2948521A1 (en)
CL (1) CL2016003062A1 (en)
EA (1) EA201650046A1 (en)
PL (1) PL415002A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113445864A (en) * 2020-03-26 2021-09-28 赛磊那实验室有限公司 Thermal insulation and sealing system for joining joints of building elements, in particular windows and access doors

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109280524A (en) * 2018-08-30 2019-01-29 山东兰桥环保建材科技有限公司 A kind of polyurethane foam glue and its preparation method and application
CN109628043A (en) * 2018-12-13 2019-04-16 重庆市天翔新材料科技有限公司 A kind of foam section protective agent is preparing the application in adhesive
CN109734867A (en) * 2018-12-19 2019-05-10 重庆市排水有限公司 The preparation method of underwater movement crack repair materials
CN109810496A (en) * 2018-12-19 2019-05-28 重庆市排水有限公司 Underwater movement crack repair materials
CN116082947B (en) * 2022-12-06 2023-09-29 石家庄东翔化工有限公司 Low-viscosity polyurethane quick-drying spray coating and preparation method and application thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE29920722U1 (en) * 1999-11-25 2000-03-02 Weiss Chemie + Technik GmbH & Co. KG, 35708 Haiger One-component PUR sealing compound
WO2001051538A1 (en) * 2000-01-13 2001-07-19 Shell Internationale Research Maatschappij B.V. Polyol formulation
PL192714B1 (en) 1997-03-20 2006-12-29 Sto Ag Assembly foam for filling joints
PL376805A1 (en) 2005-08-29 2007-03-05 Mirosław Wójcik Adhesive mortar composition
US20080038461A1 (en) * 2004-03-11 2008-02-14 Huzeir Lekovic Attached, High Reactivity Rigid Polyurethane Foams
EP1911781A1 (en) * 2006-10-12 2008-04-16 Arizona Chemical Company Oil absorbing foam
US20140045962A1 (en) * 2012-08-08 2014-02-13 Karl-Heinz Schofalvi Impact absorbing foam
US20140162006A1 (en) * 2011-07-18 2014-06-12 Bayer Intellectual Property Gmbh Water-blown pur/pir rigid foam material that can be sprayed

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6288133B1 (en) * 1997-09-10 2001-09-11 H. B. Fuller Licensing & Financing Inc. Foaming urethane composition and methods of using such compositions
CA2817556C (en) * 2010-11-17 2014-12-30 Fomo Products, Inc. Method for filling wall cavities with expanding foam insulation
PE20150183A1 (en) * 2012-07-04 2015-02-12 Basf Se PRODUCTION OF FOAMS THAT HAVE BETTER PROPERTIES
CN103910854B (en) * 2013-01-05 2016-02-24 万华化学(北京)有限公司 Fire-retardant semi-hard polyurethane foam of a kind of low density and preparation method thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL192714B1 (en) 1997-03-20 2006-12-29 Sto Ag Assembly foam for filling joints
DE29920722U1 (en) * 1999-11-25 2000-03-02 Weiss Chemie + Technik GmbH & Co. KG, 35708 Haiger One-component PUR sealing compound
WO2001051538A1 (en) * 2000-01-13 2001-07-19 Shell Internationale Research Maatschappij B.V. Polyol formulation
US20080038461A1 (en) * 2004-03-11 2008-02-14 Huzeir Lekovic Attached, High Reactivity Rigid Polyurethane Foams
PL376805A1 (en) 2005-08-29 2007-03-05 Mirosław Wójcik Adhesive mortar composition
EP1911781A1 (en) * 2006-10-12 2008-04-16 Arizona Chemical Company Oil absorbing foam
US20140162006A1 (en) * 2011-07-18 2014-06-12 Bayer Intellectual Property Gmbh Water-blown pur/pir rigid foam material that can be sprayed
US20140045962A1 (en) * 2012-08-08 2014-02-13 Karl-Heinz Schofalvi Impact absorbing foam

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113445864A (en) * 2020-03-26 2021-09-28 赛磊那实验室有限公司 Thermal insulation and sealing system for joining joints of building elements, in particular windows and access doors
EP3885521A1 (en) * 2020-03-26 2021-09-29 SELENA LABS Sp.z o.o. Sealing system for joints of joinery construction elements

Also Published As

Publication number Publication date
EA201650046A1 (en) 2017-07-31
US20170152363A1 (en) 2017-06-01
CA2948521A1 (en) 2017-06-01
AR106871A1 (en) 2018-02-28
BR102016027643A2 (en) 2017-07-18
CL2016003062A1 (en) 2017-08-04
PL415002A1 (en) 2017-06-05
CN106810662A (en) 2017-06-09

Similar Documents

Publication Publication Date Title
EP3176195A1 (en) Mounting foam and its application as an adhesive, sealant, to make coatings or to fill void structures inside
ES2651451T3 (en) Fire Barrier Panel
PT1516720E (en) Composite element comprising a polyurethane adhesion promoter
ES2913842T3 (en) Composite material elements made from thermal insulation material, adhesive and coating layer
EP3132099A1 (en) Panel with fire barrier
JP7366898B2 (en) Polyurethane-based insulation board
TW200904869A (en) Polymer foam and foam articles for fire protection
WO2006010697A1 (en) Polyisocyanate and aqueous alkali silicate based coating formulation for use in sandwich panels
RU2759184C9 (en) Reinforced sandwich panels
JP2901537B2 (en) Inorganic-organic composite foam and method for producing the same
KR20120090032A (en) Method for producing flameproof (rigid) pur spray foams
JP7216727B2 (en) Glass fiber reinforced polyurethane/polyisocyanurate foam insulation board
CN109415481A (en) The method for manufacturing sandwich component
JP7258879B2 (en) Polyurethane insulation board
KR100872439B1 (en) Fire proofing method for steel frame
CN114196364A (en) Polyurethane foaming adhesive and preparation method and application thereof
JP2915797B2 (en) Foam thickening makeup structure and foam thickening makeup method
CN114891478A (en) Preparation method and application of low-sag solvent-free polyurethane adhesive
JP3148680B2 (en) Manufacturing method of inorganic-organic composite foam
JPH10195225A (en) Inorganic and organic composite foam and its production
JPH11180783A (en) Inorganic organic combined formed body and its production
JPH1067877A (en) Inorganic-organic composite foam and its production
JPH11180782A (en) Inorganic-organic combined expanded body and its production
JPH1129648A (en) Inorganic and organic composite foamed product and its production
JPH11181137A (en) Inorganic/organic composite foam and its production

Legal Events

Date Code Title Description
AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20171207

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

17Q First examination report despatched

Effective date: 20181128

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20190409